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浓度依赖性剪接由中等亲和力的 Rbfox 基序介导。

Concentration-dependent splicing is enabled by Rbfox motifs of intermediate affinity.

机构信息

Department of Biology, Massachusetts Institute of Technology, Cambridge, MA, USA.

出版信息

Nat Struct Mol Biol. 2020 Oct;27(10):901-912. doi: 10.1038/s41594-020-0475-8. Epub 2020 Aug 17.

Abstract

The Rbfox family of splicing factors regulate alternative splicing during animal development and in disease, impacting thousands of exons in the maturing brain, heart and muscle. Rbfox proteins have long been known to bind to the RNA sequence GCAUG with high affinity and specificity, but just half of Rbfox binding sites contain a GCAUG motif in vivo. We incubated recombinant RBFOX2 with over 60,000 mouse and human transcriptomic sequences to reveal substantial binding to several moderate-affinity, non-GCAYG sites at a physiologically relevant range of RBFOX2 concentrations. We find that these 'secondary motifs' bind Rbfox robustly in cells and that several together can exert regulation comparable to GCAUG in a trichromatic splicing reporter assay. Furthermore, secondary motifs regulate RNA splicing in neuronal development and in neuronal subtypes where cellular Rbfox concentrations are highest, enabling a second wave of splicing changes as Rbfox levels increase.

摘要

Rbfox 家族剪接因子在动物发育和疾病过程中调节可变剪接,影响成熟大脑、心脏和肌肉中数千个外显子。Rbfox 蛋白长期以来一直被认为能够与 RNA 序列 GCAUG 高度特异性结合,但在体内,只有一半的 Rbfox 结合位点含有 GCAUG 基序。我们用超过 60000 个小鼠和人类转录组序列孵育重组 RBFOX2,揭示了在生理相关的 RBFOX2 浓度范围内对几个中等亲和力、非 GCAYG 结合位点的大量结合。我们发现这些“次要基序”在细胞中能够强烈结合 Rbfox,并且几个结合位点一起可以在三色剪接报告基因检测中发挥与 GCAUG 相当的调节作用。此外,次要基序在神经元发育和神经元亚型中调节 RNA 剪接,在这些亚型中细胞 Rbfox 浓度最高,使得随着 Rbfox 水平的增加,出现了第二波剪接变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6523/7554199/2467b6cb5266/nihms-1608569-f0007.jpg

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